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AMT

aminomethyltransferase

gene with protein productOMIM: 2383103 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in3
Atypical glycine encephalopathyORPHA:289863
→
Neonatal glycine encephalopathyORPHA:289857
→
Infantile glycine encephalopathyORPHA:289860
→
Данные: Orphadata (CC-BY-4.0)